Patients Ulcerative colitis
Recently diagnosed and terrified
- 36 views
- 3 times supported
- 2 comments
Hello everyone, I am a 22 year old college student who was just diagnosed with Ulcerative Colitis, three days ago. I have yet to meet with my doctor (he's given me medication and we'll meet back in a month) but I have no idea what I am doing. I went online for answers and now, I'm terrified. Luckily, the disease hasn't spread much but, I'm still scared ill wake up and my entire large intestine will need to be removed. I'm scared to eat, talk about it and basically every other normal day activity.
Please send some advice. I'd greatly appreciate it. Thank you!
@22Knop Hello 22Knop, thank you for opening this discussion and sharing what you're going through. Getting diagnosed with a chronic disease like ulcerative colitis can be overwhelming and stressful. Let me tag some other members of our community who can possibly share some advice with you!
Hi everyone, how are you doing?
Do you remember how you felt when you were diagnosed? Were you scared, stressed, confused, or were you able to accept it? Can you share some advice with 22Knop? What would you like to have known when you were diagnosed?
@Ohhhdalia @Conicam @DeborahCosentino @mvvssaa @amackay @LoriParry @Lala1124 @GoldenUmassJoe @Saram01 @dorentin97 @Mineira100 @7042021999 @Debhandy @bassgreg @Kowen94 @MKearns @Sheila70
Feel free to share here, we're all here to support one another!
See the signature
Courtney_J, Community Manager, Carenity US
Thank you for being open about your diagnosis.
My name is Anthony I was diagnosed in 2016 at the age of 30, after about a year of going to the bathroom 20-40 times a day, weight loss and bleeding (you will get comfortable with being open about this, I was terrified because of the stigma of "bathroom talk".) I had no idea what it was, I was a college athlete wondering why, what did I do. First thing is you need to know is, it's not your fault. I was very scared after looking at web MD and all the internet talk, what made me comfortable was talking to people who have had the diagnosis for 30, 40 even 50 years. I have a very mild case and am lucky but I recently just kicked my 2nd flare in 5 years, what I have found most draining is the mental aspect of this and its not really talked about with the disease. Please reach out and there is help, you are not alone. Anthony
See the signature
Give your opinion
Members are also commenting on...
Articles to discover...
07/24/2023 | News
07/12/2023 | Testimonial
05/19/2023 | Advice
02/12/2019 | Advice
04/08/2019 | Advice
05/13/2019 | Advice
05/05/2020 | News
You wish to be notified of new comments
You have been subscribed